Do you want to help ensure quality in Life Science together with the sharpest minds in the industry? Then this is where you should be. With us, you'll find assignments that require curiosity, drive for solutions and sharp expertise, and that give you the chance to develop in new contexts. Together we contribute to a better tomorrow and shape future solutions that make a difference for people and society.
This is your role
You will become part of our Life Science Compliance business area and the Quality & Validation unit – which consists of 6 teams with broad expertise in quality, validation and production.
As a consultant with us, you work on varying assignments where you get the opportunity to quickly build experience and develop in several areas you are passionate about.
Examples of what you can work with:
Validation, qualification and commissioning of equipment, systems and processes.
Improvement work within manufacturing and work processes.
Improve our customers' quality management systems.
Roles as quality or process engineer, validation engineer/manager or sub-project manager.
You have your own responsibility in your assignments, but never alone – you always have the support of a team with senior expertise to consult with.
We have offices at several locations in Sweden, this position is located at our office in Kista.
Why you'll thrive as a consultant with us
Here you get the best of the consultant role:
Variety – different assignments, techniques and operations
Rapid development – a steep learning curve where you build both breadth and depth
Impact – you are part of driving improvement and quality at our customers
We are at the forefront of our field and work as an advisory partner. This is evident from the fact that we:
Drive complex and developmental projects at our customers
Educate and lecture in our specialist areas
Actively share knowledge – both internally and externally
With us, you are always part of a context – a team where we learn from each other and where senior colleagues contribute to your development.
How you will excel
You are curious, solution-oriented and thrive in a role where you can take responsibility and collaborate with others. You build trust, communicate clearly and have a strong focus on quality.
We believe you have:
At least 3 years of experience from GMP/GxP-regulated operations within Pharma/Biotech
Higher education or engineering degree in technology or natural sciences
Experience in validation or technical production, preferably combined with a strong interest in quality and problem-solving
Ability to work systematically and drive work forward
Very good knowledge of Swedish and English
Being part of Team PV
With us you get something different.
We don't recruit for a specific assignment – we recruit to build our team long-term. This means we look at you, your expertise and your development over time, and create the right conditions for you to continue to grow.
We work as an advisory partner to our customers and value long-term relationships – both externally and internally. In the team there is a strong culture of knowledge sharing, where consultants learn from each other and contribute to the whole.
Our culture is something we are genuinely proud of. We are a Great Place to Work, year after year – and see it as proof of the environment we build together every day.
And yes – if our culture were in the walls, they would be soft.
Application
During the holiday period, it may take a while before you hear from us, selection and interviews will begin as soon as possible after the vacation. If you have questions about this position, feel free to contact Ida Holmberg at 076 - 108 84 87, [email protected].
Welcome with your application!
Do you have your own company and are interested in collaborating with us as a sub-consultant?
Instead of applying for a specific position, please connect with us via our careers page and indicate that you are interested in working as a sub-consultant – and we'll get in touch when something suitable comes up.Do you want to help ensure quality in Life Science together with the sharpest minds in the industry? Then this is where you should be. With us, you'll find assignments that require curiosity, drive for solutions and sharp expertise, and that give you the chance to develop in new contexts. Together we contribute to a better tomorrow and shape future solutions that make a difference for people and society.
This is your role
You will become part of our Life Science Compliance business area and the Quality & Validation unit – which consists of 6 teams with broad expertise in quality, validation…